코스넷:::::화장품원료:::::

 ▣ 천연물에서 분리된 개별유효성분 레코드 등록정보

성 분 명 

Epilupinine

다른이름들 

Isolupinine

함유 천연물 

Sophora secundiflora (Ortega) Lag.ex DC.[]()
Sophora tomentosa L.[-]()

분 자 식 

C₁₀H₁₉NO

화학족 분류 

알칼로이드(alkaloid);

분 자 량 

169.269

녹 는 점 

79.5-80.5°C

HNMR_CHART 

(CDCl3) δ:3.65(1H, dd), 3.55(1H, dd), 2.81(2H, br t), 1.1-2.1(14H, m)

MASS_CHART 

GCM+= 169, m/z= 168, 152, 138, 124, 111, 110, 97, 83(100), 55

참고문헌 

· PA. Grieco et al., J. Org. Chem., 53, 3325, 1988(ir,pmr) · EP. White, N. Z. J. Sci. Technol., Sect. B, 33, 50, 1951 · WD. Crow et al., Aust. J. Chem., 8, 136, 1955; 10, 77, 1957 · AF. Thomas et al., Can. J. Chem., 33, 1290, 1955 · EE. Van Tamelen et al., J. Am. Chem. Soc., 82, 502, 1960 · S. Paszyc et al., Bull. Acad. Pol. Sci., Ser. Sci. Chim., 18, 15, 1970 · V. Batra et al., Indian J. Chem., Sect. B, 14, 636, 1976 · AB. Beck et al., J. Nat. Prod., 42, 385, 1979 · M. Okita et al., Heterocycles, 20, 401, 1983 · ML. Bremmer et al., J. Org. Chem., 48, 3661, 1983 · AR. Chamberlin et al., J. Org. Chem., 49, 1682, 1984 · M. Ihara et al., Heterocycles, 23, 1097, 1985 · H. Hiemstra et al., J. Org. Chem., 50, 4014, 1985 · H. Takahata et al., Chem. Pharm. Bull., 34, 4523, 1986 · T. Nagasaka et al., Heterocycles, 29, 1209, 1989 · JP. Celerier et al., Tetrahedron, 45, 6161, 1989 · S. Takamatsu et al., Phytochemistry, 29, 3923, 1990 · S. Takamatsu et al., J. Nat. Prod., 54, 477, 1991 · DH. Hua et al., Synthesis, 970, 1991 · ED. Edstrom, Tetrahedron Lett., 32, 5709, 1991 · JP. Gesson et al., Tetrahedron Lett., 33, 3633, 1992 · G. Pandey et al., Tetrahedron Lett., 33, 6533, 1992 · FG. West et al., J. Am. Chem. Soc., 116, 8420, 1994 · H. Suzuki et al., Phytochemistry, 37, 591, 1994